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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7061433inversion1nstd229human GRCh38 chr16: 19,893,387-21,501,582 , GRCh37.p13 chr16: 19,904,709-21,512,903 CRYM, SNX29P1, 38 more genes
    nsv6997825copy number variation1nstd229human GRCh38 chr16: 20,768,059-20,856,206 , GRCh37.p13 chr16: 20,779,381-20,867,528 RNU6-944P, DCUN1D3, 4 more genes
    nsv6990386copy number variation1nstd229human GRCh38 chr16: 20,883,278-20,887,080 , GRCh37.p13 chr16: 20,894,600-20,898,402 DCUN1D3
    nsv6988106copy number variation1nstd229human GRCh38 chr16: 20,867,922-20,869,035 , GRCh37.p13 chr16: 20,879,244-20,880,357 DCUN1D3
    nsv6987331copy number variation1nstd229human GRCh38 chr16: 20,899,915-21,180,228 , GRCh37.p13 chr16: 20,911,237-21,191,549 LDAF1, LYRM1, 3 more genes
    nsv6985682copy number variation1nstd229human GRCh38 chr16: 20,882,901-20,891,600 , GRCh37.p13 chr16: 20,894,223-20,902,922 DCUN1D3
    nsv6985391copy number variation1nstd229human GRCh38 chr16: 20,826,994-20,856,200 , GRCh37.p13 chr16: 20,838,316-20,867,522 DCUN1D3, REXO5, 1 more genes
    nsv6979844copy number variation1nstd229human GRCh38 chr16: 20,865,870-20,874,842 , GRCh37.p13 chr16: 20,877,192-20,886,164 DCUN1D3
    nsv6978791copy number variation1nstd229human GRCh38 chr16: 20,872,521-20,872,626 , GRCh37.p13 chr16: 20,883,843-20,883,948 DCUN1D3
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6514717copy number variation1nstd223human GRCh38 chr16: 20,768,058-20,856,205 , GRCh37.p13 chr16: 20,779,380-20,867,527 ACSM3, REXO5, 4 more genes
    nsv6514199copy number variation1nstd223human GRCh38 chr16: 20,883,278-20,887,042 , GRCh37.p13 chr16: 20,894,600-20,898,364 DCUN1D3
    nsv6500838copy number variation1nstd223human GRCh38 chr16: 20,882,901-20,891,700 , GRCh37.p13 chr16: 20,894,223-20,903,022 DCUN1D3
    nsv6499642copy number variation1nstd223human GRCh38 chr16: 20,872,533-20,873,924 , GRCh37.p13 chr16: 20,883,855-20,885,246 DCUN1D3
    nsv6133261copy number variation1nstd213human GRCh37 chr16: 19,140,000-21,360,001 , GRCh38.p12 chr16: 19,128,678-21,348,680 CRYM, GP2, 49 more genes
    nsv6133258copy number variation1nstd213human GRCh37 chr16: 16,530,000-21,500,001 , GRCh38.p12 chr16: 16,436,143-21,488,680 CRYM, GP2, 93 more genes
    nsv6133013copy number variation1nstd213human GRCh37 chr16: 19,620,000-22,460,001 , GRCh38.p12 chr16: 19,608,678-22,448,680 CDR2, CRYM, 76 more genes
    nsv6037373copy number variation1nstd212human GRCh38 chr16: 20,861,302-20,861,371 , GRCh37.p13 chr16: 20,872,624-20,872,693 DCUN1D3
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
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